Chlordane exposure impairs the growth and behavior of Drosophila.

Chlordane, a previously extensively utilized insecticidal pesticide, has since been prohibited, however, owing to its limited degradability, it continues to persist significantly in soil and water reservoirs, subsequently accumulating within plant and animal organisms, representing a substantial threat to human health. Despite extensive research conducted over the past few decades to investigate the toxic effects of chlordane, there remains a notable dearth of studies focusing on its impact on sleep activity. Therefore, in this study, the effects of short-term and long-term exposure to chlordane on the activity and sleep of Drosophila were investigated. When exposed to chlordane at a concentration of 1 µM, Drosophila lost body weight, decreased body size and resulted in lipid metabolism disorders. In addition, chlordane exposure altered the arousal and sleep behaviors of Drosophila. Short-term exposure to chlordane resulted in an increase in night-time sleep duration, while long-term exposure to chlordane resulted in an increase in activity and a decrease in sleep, as evidenced by a decrease in the duration of each sleep session and the appearance of sleep fragmentation. Under conditions of long-term chlordane exposure, reactive oxygen species levels were significantly up-regulated in Drosophila. Our results suggest that long-term chlordane exposure triggers oxidative stress damage in Drosophila, leading to sleep disruption. This study offers novel insights into the harmful impacts of environmental pollutants on human sleep patterns and proposes that mitigating the presence of chlordane in the environment could potentially contribute to the reduction of global sleep disorder prevalence.

Application of hollow fiber-protected liquid-phase microextraction combined with GC-MS in determining Endrin, Chlordane, and Dieldrin in rice samples.

This paper introduces a novel and minimized sample preparation technique based on hollow fiber-protected liquid-phase microextraction that can be used in joint with gas chromatography-mass spectrometry (GC-MS) detection to extract three organochlorine pesticides-Endrin, Chlordane, and Dieldrin-from rice samples. To that end, a single-walled carbon nanotube (SWCNT) and a proper ionic liquid (IL) were ultrasonically dispersed and injected into the lumen of hollow fiber as the extraction phase for preconcentrating and extracting the target analytes from the rice samples. The effects of the type of nanoparticles, ILs, and desorption solvent on the efficiency of extracting the analytes were investigated based on the one-factor-at-a-time (OFAT) approach. In addition, other parameters influencing the extraction procedure were optimized using an experimental design that decreased the number of experiments, reagent consumption, and costs. Under optimized conditions, the limits of detection and quantification in determining mentioned pesticides varied between 0.019-0.029 and 0.064-0.098 ng mL-1, respectively. The calibration graphs to measure Endrin, Chlordane, and Dieldrin were linear over the concentration range of 0.064-13.2, 0.098-16.7, and 0.092-11.4 ng mL-1, respectively. The relative standard deviations for inter-day and intra-day analysis were below 7.06 and 4.75% for the triplicate determination of three organochlorine pesticides. Besides, the relative recoveries and standard deviations of Endrin, Chlordane, and Dieldrin for analyzing several Iranian rice samples were between 86.0-92.9% and 4.5-5.8%, respectively. The results were compared with other similar works in literature, proving that the proposed method is efficient and useful for routine monitoring of organochlorine compounds in food samples.

Chlorinated persistent organic pollutants in human breast milk in the Miyagi Prefecture disaster-affected area 1 year after the Great East Japan Earthquake of 2011.

BACKGROUND: In the Great East Japan Earthquake of 11 March 2011, an earthquake and accompanying tsunami struck the Tohoku region of northeastern Japan. Buildings collapsed and the tsunami spread waste, including hazardous materials. This study aimed to determine the concentrations of persistent organic pollutants (POPs) in the breast milk of mothers living in the disaster-affected area of Sendai 1 year after the earthquake. Temporal trends in the POPs concentrations were evaluated by comparison with previous studies. METHODS: One hundred breast milk samples were obtained from lactating mothers at a hospital in Sendai in 2012. The results were compared with those from other years to examine whether there were changes in the POPs concentrations after the earthquake. We measured polychlorinated biphenyls (PCBs) and organochlorine pesticides, such as chlordanes, using gas chromatography-mass spectrometer (GC-MS) with negative chemical ionization, and dichlorodiphenyl trichloroethane (DDT) and its metabolites using GC-MS with electron impact ionization. RESULTS: The mean total PCBs (11 congeners), total chlordane, and total DDT concentrations were 76.2 ng/g lipid, 39.8 ng/g lipid, and 73.5 ng/g lipid, respectively. For the samples collected in 2012, the concentrations of POPs in breast milk showed minimal changes compared with results from previous years for samples collected at the same hospital in Sendai. CONCLUSIONS: Our study demonstrates that 1 year after the earthquake and tsunami, the concentrations of chlorinated POPs in breast milk had not changed substantially.

DDT, Chlordane, and Hexachlorobenzene in the Air of the Pearl River Delta Revisited: A Tale of Source, History, and Monsoon.

Although organochlorine pesticides (OCPs) have been banned for more than three decades, their concentrations have only decreased gradually. This may be largely attributable to their environmental persistence, illegal application, and exemption usage. This study assessed the historic and current regional context for dichlorodiphenyltrichloroethane (DDT), chlordane, and hexachlorobenzene (HCB), which were added to the Stockholm Convention in 2001. An air sampling campaign was carried out in 2018 in nine cities of the Pearl River Delta (PRD), where the historical OCP application was the most intensive in China. Different seasonalities were observed: DDT exhibited higher concentrations in summer than in winter; chlordane showed less seasonal variation, whereas HCB was higher in winter. The unique coupling of summer monsoon with DDT-infused paint usage, winter monsoon with HCB-combustion emission, and local chlordane emission jointly presents a dynamic picture of these OCPs in the PRD air. We used the BETR Global model to back-calculate annual local emissions, which accounted for insignificant contributions to the nationally documented production (<1‰). Local emissions were the main sources of p,p'-DDT and chlordane, while ocean sources were limited (<4%). This study shows that geographic-anthropogenic factors, including source, history, and air circulation pattern, combine to affect the regional fate of OCP compounds.

Exposure to organochlorine pesticides and the risk of type 2 diabetes in the population of East China.

Organochlorine pesticides (OCPs) have been reported to be associated with an elevated risk of type 2 diabetes, although no study has focused on such associations in Chinese populations. In this case-control study, we aimed to explore the associations between OCPs and type 2 diabetes and their potential mechanisms in a population from East China. Participants diagnosed with type 2 diabetes and nondiabetic participants from Shandong Province, East China, were enrolled in this case-control study. Six OCPs (ß-HCH, trans-chlordane, trans-nonachlor, p,p'-DDE, p,p'-DDT and mirex/kepone) were detected in more than 75% of serum samples. Logistic regression analysis and multiple linear regression analysis were used to assess the associations between OCP exposure and the outcomes. After adjusting for potential confounding factors such as age, sex and body mass index, all six OCPs showed positive associations with type 2 diabetes in a linear dose-response manner. Serum concentrations of ß-HCH and p,p'-DDE were associated with higher levels of fasting plasma glucose in participants without diabetes, although no OCPs showed significant associations with hemoglobin A1c. In addition, certain OCPs showed significantly positive associations with triglycerides, total cholesterol, and low-density lipoprotein cholesterol and negative relationships with high-density lipoprotein cholesterol in nondiabetics, indicating that OCP exposure may disrupt lipid metabolism. Findings in the current study indicated that OCPs may be a diabetogenic factor in the population of this study. To our knowledge, this is the first study to investigate the associations between OCP exposure and type 2 diabetes in a Chinese population.

20 Years of Air-Water Gas Exchange Observations for Pesticides in the Western Arctic Ocean.

The Arctic has been contaminated by legacy organochlorine pesticides (OCPs) and currently used pesticides (CUPs) through atmospheric transport and oceanic currents. Here we report the time trends and air-water exchange of OCPs and CUPs from research expeditions conducted between 1993 and 2013. Compounds determined in both air and water were trans- and cis-chlordanes (TC, CC), trans- and cis-nonachlors (TN, CN), heptachlor exo-epoxide (HEPX), dieldrin (DIEL), chlorobornanes (ΣCHBs and toxaphene), dacthal (DAC), endosulfans and metabolite endosulfan sulfate (ENDO-I, ENDO-II, and ENDO SUL), chlorothalonil (CHT), chlorpyrifos (CPF), and trifluralin (TFN). Pentachloronitrobenzene (PCNB and quintozene) and its soil metabolite pentachlorothianisole (PCTA) were also found in air. Concentrations of most OCPs declined in surface water, whereas some CUPs increased (ENDO-I, CHT, and TFN) or showed no significant change (CPF and DAC), and most compounds declined in air. Chlordane compound fractions TC/(TC + CC) and TC/(TC + CC + TN) decreased in water and air, while CC/(TC + CC + TN) increased. TN/(TC + CC + TN) also increased in air and slightly, but not significantly, in water. These changes suggest selective removal of more labile TC and/or a shift in chlordane sources. Water-air fugacity ratios indicated net volatilization (FR > 1.0) or near equilibrium (FR not significantly different from 1.0) for most OCPs but net deposition (FR < 1.0) for ΣCHBs. Net deposition was shown for ENDO-I on all expeditions, while the net exchange direction of other CUPs varied. Understanding the processes and current state of air-surface exchange helps to interpret environmental exposure and evaluate the effectiveness of international protocols and provides insights for the environmental fate of new and emerging chemicals.

Persistent organochlorines in 13 shark species from offshore and coastal waters of Korea: Species-specific accumulation and contributing factors.

Data on persistent organochlorines (OCs) in sharks are scarce. Concentrations of OCs such as polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in the muscle tissue of 13 shark species (n=105) collected from offshore (Indian and Pacific Oceans) and coastal waters of Korea, to investigate species-specific accumulation of OCs and to assess the potential health risks associated with consumption of shark meat. Overall OC concentrations were highly variable not only among species but also within the same species of shark. The concentrations of PCBs, DDTs, chlordanes, hexachlorobenzene, and heptachlor in all shark species ranged from

Estimation of human health risk associated with the consumption of pesticide-contaminated vegetables from Kumasi, Ghana.

Analysis of pesticides consisting of 12 organophosphates (OPs), 10 organochlorines (OCs), and 6 pyrethroids in vegetables from Kumasi was conducted. Vegetable samples comprising 20 each of eggplants, okra, and tomatoes were analyzed. The method involves solvent extraction of pesticide residues followed by cleanup using silica gel. Residue analysis was carried out using a GC equipped with pulsed flame photometric detector for OP residues and electron capture detector for OC and pyrethroid residues. The results revealed that methamidophos exceeded the maximum residue limits (MRLs) in all vegetable commodities. Levels of malathion and dimethoate also exceeded the MRLs in eggplant and tomato samples. Endrin, α-endosulfan, γ-hexachlorocyclohexane (HCH), γ-chlordane, and heptachlor exceeded their MRLs in okra samples whereas methoxychlor, allethrin, and deltamethrin exceeded in eggplant samples. Health risk estimation revealed that dimethoate in tomato and endrin, heptachlor, γ-HCH, and γ-chlordane in okra could not pose potential toxicity to the consumer. The combined risk index showed no health risk to consumers due to intake of pyrethroid OC and OP residue on these vegetables. The overall risk index for combined pesticides due to consumption of all the vegetables was higher than 1, which signifies potential health risk to consumers. OPs were the major risk contributor for both eggplant and tomatoes which accounted for 87.78 and 95.84%, respectively, of the combined risk of pesticides in the vegetables. However, OC with 97.94% of the combined risk index was the major risk contributor for the okra. The carcinogenic risk of the OCs in okra was of no concern since their carcinogenic rates were below the acceptable risk level.

Enantiomer-selective and quantitative trace analysis of selected persistent organic pollutants (POP) in traditional food from western Greenland.

Enantiomeric fractions (EF) are today considered a powerful tool to elucidate selective uptake processes of chiral contaminants in biota. In this study, concentration levels and EF were determined by gas chromatograph-mass spectrometer (GC/MS) for α-hexachlorocyclohexane (α-HCH) and trans-, cis-, and oxychlordane in selected Greenlandic traditional food items, collected at the local market in Nuuk in 2010. The food items selected were raw and smoked fish (salmon and halibut, n = 6), whale meat (n = 8), seal meat (n = 2) and narwhal mattak (skin and blubber, n = 6). The EF were nonracemic (≠0.5) for all samples except for α-HCH in narwhal, trans-chlordane in whale and smoked salmon, and cis- and oxychlordane in seal. The EF for α-HCH were significant for all fish samples, but not for mammalian samples. Data indicate that different uptake and/or transformation mechanisms may be responsible for nonracemic distributions of chiral pesticides in mammals and fish species analyzed. There were no general enantiomer-selective transformation/accumulation trends found for chlordanes. Data indicate that enantiomer-specific properties are an important prerequisite for interaction of chiral contaminant with internal metabolic processes. However, marked differences within these groups were identified. The EF in ringed seals were racemic for most of the analyzed pesticides (i.e., chlordanes). However, narwhal were characterized by nonracemic EF for all chiral pesticides analyzed. Median levels of α-HCH ranged from 2 to 24 ng/g lw and from 15.1 to 626.6 ng/g lw for trans-nonachlor, with lowest levels observed in smoked salmon and highest levels in narwhal mattak. This study confirmed that concentration levels of analyzed pesticides in the investigated food items were below the tolerable daily intake (TDI) threshold.

Sixty-year sedimentary record of DDTs, HCHs, CHLs and endosulfan from emerging development gulfs: a case study in the Beibu Gulf, South China Sea.

The temporal distribution of organochlorine pesticides (OCPs) was examined in the (210)Pb dated sediment core from the Beibu Gulf, South China Sea. The total OCPs concentrations were in the range of 0.93-26.6 ng g(-1) dry weight. Dichlorodiphenyltrichloroethanes (DDTs) (0.17-24.8 ng g(-1)), Hexachlorocyclohexanes (HCHs) (0.04-0.51 ng g(-1)), Chlordane related compounds (CHLs) (0.22-1.72 ng g(-1)) and endosulfan (n.d.-0.91 ng g(-1)) were the predominant compounds. Similar to most Chinese coastal areas, the levels of DDTs in the Beibu Gulf became elevated since the early 1990s, especially since 2000 despite the ban in 1983 in China. This suggests that the concentrations of DDTs were controlled by several processes, such as land reclamation and soil runoff. The isomer ratios of (p,p'-DDE + p,p'-DDD)/p,p'-DDT, p,p'-DDT/DDTs along with construction land expansion indicated that economic activities, land reclamation, soil runoff and the use of DDT-containing antifouling paints might be responsible for the input of DDT. The ratios of α-HCH/γ-HCH (and γ-HCH/HCHs) and trans-chlordane/cis-chlordane (TC/CC) indicated fresh inputs of lindane and chlordane, respectively. In addition, CC was found to be degraded faster than TC under anaerobic conditions in sediments from the Beibu Gulf.

Multiple lines of evidence point to pesticides as stressors affecting invertebrate communities in small streams in five United States regions.

Multistressor studies were performed in five regions of the United States to assess the role of pesticides as stressors affecting invertebrate communities in wadable streams. Pesticides and other chemical and physical stressors were measured in 75 to 99 streams per region for 4 weeks, after which invertebrate communities were surveyed (435 total sites). Pesticides were sampled weekly in filtered water, and once in bed sediment. The role of pesticides as a stressor to invertebrate communities was assessed by evaluating multiple lines of evidence: toxicity predictions based on measured pesticide concentrations, multivariate models and other statistical analyses, and previously published mesocosm experiments. Toxicity predictions using benchmarks and species sensitivity distributions and statistical correlations suggested that pesticides were present at high enough concentrations to adversely affect invertebrate communities at the regional scale. Two undirected techniques-boosted regression tree models and distance-based linear models-identified which pesticides were predictors of (respectively) invertebrate metrics and community composition. To put insecticides in context with known, influential covariates of invertebrate response, generalized additive models were used to identify which individual pesticide(s) were important predictors of invertebrate community condition in each region, after accounting for natural covariates. Four insecticides were identified as stressors to invertebrate communities at the regional scale: bifenthrin, chlordane, fipronil and its degradates, and imidacloprid. Fipronil was particularly important in the Southeast region, and imidacloprid, bifenthrin, and chlordane were important in multiple regions. For imidacloprid, bifenthrin, and fipronil, toxicity predictions were supported by mesocosm experiments that demonstrated adverse effects on naïve aquatic communities when dosed under controlled conditions. These multiple lines of evidence do not prove causality-which is challenging in the field under multistressor conditions-but they make a strong case for the role of insecticides as stressors adversely affecting invertebrate communities in streams within the five sampled regions.

Spatial and interspecific patterns in persistent contaminant loads in bighead and silver carp from the Illinois River.

We measured concentrations of selected organohalogens, fluorinated compounds and mercury in whole, ground silver (Hypophthalmichthys molitrix) and bighead (H. nobilis) carp from the Illinois River, Illinois, in 2010 and 2011 to characterize spatial and interspecific patterns of contaminant burdens. Silver carp, which had greater lipid content, tended to have greater concentrations of lipophilic compounds. Concentrations of organohalogens were generally greater in carp from the upper reaches of the river. The halogenated compounds were associated with length and lipid content in silver carp. Bighead carp had greater mercury concentrations than did silver carp; total mercury concentrations were negatively associated with lipid content of bighead carp. Perfluorinated compounds, comprised predominantly of perfluorooctane sulfonic acid, did not vary by species or river reach. Chlordanes and polychlorinated biphenyls were of potential concern with regard to the use of these carp as animal feed additives. Our results indicated that, even though they occupy a lower trophic level than many similarly-sized fish, these carp may accumulate measureable concentrations of organic contaminants.

OCPs and PCBs in marine edible fish and human health risk assessment in the eastern Guangdong, China.

Marine edible fish samples were collected from two important nearshore fishing sites in the eastern Guangdong Province, China: Shantou Harbor and Haimen Bay. In the mixed edible muscle tissues of marine fish samples, the concentrations of polychlorinated biphenyls, dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), chlordanes, and hexachlorobenzene ranged from 1.12 to 53.87, ND (not detected) to 84.01, 0.22 to 7.09, ND to 4.74, and ND to 1.49 ng/g wet weight (ww) in Haimen Bay, respectively, and from ND to 70.35, ND to 164.83, ND to 8.68, ND to 25.61, and ND to 1.76 ng/g ww in Shantou Harbor, respectively. The concentrations of PCBs, DDTs, and HCHs in all samples did not exceed maximum residue limits (China and United States Food and Drug Administration). However, a few fish samples exceed the maximum levels established by the European Union. Daily fish consumption from this region can be of serious concern, and lifetime cancer risk remains a possibility in the studied area.

Nationwide assessment of atmospheric organochlorine pesticides over a decade during 2008-2017 in South Korea.

Long-term nationwide atmospheric monitoring of organochlorine pesticides (OCPs) was performed in South Korea during 2008-2017. Their occurrences, seasonal and temporal variability, sources, and effect of ambient temperature were investigated. The OCPs are pronounced with a mean concentration of total OCPs ranging from 5.2 to 256 pg/Sm3. However, a decrease of 54 % was observed in the mean concentration of total OCPs from 2008 to 2017 associated with regulatory actions. OCP concentrations did not show any variations between the different site types, and OCPs were ubiquitously present at all site types. The mean concentration of total OCPs in summer was two-fold higher than in winter. The concentrations of DRINs, DDTs, ENDOs, and HCHs were significantly higher in summer, but the concentrations of chlordane and heptachlor were higher in winter. The diagnostic ratios identified major sources as ongoing sources, past use, and atmospheric transport. Clausius Clapeyron plots strongly suggested the re-emission of α-endosulfan, ß-endosulfan, α-HCH, and ß-HCH, and ΔHsa (enthalpy of surface air exchange) values suggested the influence of the transport and/or new sources on aldrin, dieldrin, and chlordane. The occurrence of OCPs due to re-emissions, ongoing sources, and long-range atmospheric transport could be a challenge towards the complete phase-out of OCPs in South Korea.

Bioaccumulation of pesticide residue in earthworms collected from the agricultural soils of Kuttanad-a unique agroecosystem in India.

Earthworms encompass significant soil faunal biomass and have tremendous potential to provide vital ecosystem services. Earthworms are considered bioindicators of chemical contaminants and can provide early warnings of ecosystem deterioration. Studies pertaining to the accumulation of pesticide residues in earthworm in biomass in agrarian ecosystems are scarce. The Kuttanad agroecosystem (KAE), situated on the southwest coast of India, is one of the few regions globally supporting farming on land below the mean sea level. This investigation was conducted to assess the bioaccumulation of pesticide residues in earthworms from the KAE. The earthworms species Glyphidrilus annandalei collected from agricultural soils of the study area were analyzed for the presence of pesticides residues such as α-BHC, γ-BHC, atrazine, heptachlor, α-chlordane, γ-chlordane, 4,4-DDE, 4,4-DDD, 4,4-DDT, ß-endosulfan, and endrin ketone in their biomass. Analysis of the earthworm samples using a gas chromatograph revealed the presence of ten pesticide residues with notable concentrations (α-BHC, 0.36 ng/g; γ-BHC, 0.41 ng/g; heptachlor, 0.10 ng/g; atrazine, 0.89 ng/g; α-chlordane, 0.07 ng/g; γ-chlordane, 0.10 ng/g; 4,4-DDE, 0.05 ng/g; 4,4-DDD, 0.11 ng/g; 4,4-DDT, 0.31 ng/g; ß-endosulfan, 0.19 ng/g; and endrin ketone, 0.13 ng/g). Six groups of pesticide residues are ΣBHC, ΣDDT, atrazine, Σchlordane, endrin ketone, and ß-endosulfan were observed during bioaccumulation factor analysis, and the results show the following trend: atrazine > ΣBHC > ΣDDT > Σchlordane > Σendosulfan > Σendrin. As earthworms are a crucial component of this region's food chains, bioaccumulation of pesticide residues in earthworms can pause adverse consequences. Increasing trends in pesticide application in the KAE and bioaccumulation of pesticide residues in earthworm biomass can affect the entire food web.

Application of sorbent impregnated polyurethane foam (SIP) disk passive air samplers for investigating organochlorine pesticides and polybrominated diphenyl ethers at the global scale.

As part of continued efforts under the Global Atmospheric Passive Sampling (GAPS) Network to develop passive air samplers applicable to a wide-range of compounds, sorbent-impregnated polyurethane foam (SIP) disk samplers were codeployed and tested against conventional polyurethane foam (PUF) disk samplers. The SIP disk sampler has a higher sorptive capacity compared to the PUF disk sampler, due to its impregnation with ground XAD resin. The two sampler types were codeployed at 20 sites during the 2009, 3-month long spring sampling period of the GAPS Network. Air concentrations for chlordanes (trans-chlordane, cis-chlordane, and trans-nonachlor) and endosulfans (endosulfan I, endosulfan II, and endosulfan sulfate) derived from PUF disk and SIP disk samplers showed near 1:1 agreement and confirmed previous results for polychlorinated biphenyls (PCBs). Discrepancies observed for α-HCH and γ-HCH in PUF disk versus SIP disk are attributed to lack of "comparability" of the PUF and SIP data sets, due to differences in effective air sampled by the two devices caused by saturation of these higher volatility compounds in the lower capacity PUF disk samplers. Analysis of PBDEs in PUF and SIP disks showed relatively good agreement but highlighted challenges associated with high blanks levels for PBDEs. The higher capacity SIP disk samplers allowed for the analysis of pentachlorobenzene (PeCBz) and hexachlorobenzene (HCBz) and revealed a relatively uniform global distribution of these compounds. The results of this study further validate the SIP disk sampler as a complement to the PUF disk sampler, with capabilities for a broad range of POPs targeted under international POPs treaties such as the Stockholm Convention on POPs and its Global Monitoring Plan.

Apportioning variability of polycyclic aromatic hydrocarbons (PAHs) and chlordanes in indoor and outdoor environments.

Measurements of semi-volatile organic compounds (SVOCs) in air are subject to substantial variability and uncertainty. This study apportions total variance of polycyclic aromatic hydrocarbons (PAHs) and chlordanes to variability and uncertainty components. Concentrations of PAHs and chlordanes were measured inside and outside of 116 residences in three large cities in the U.S. during 1999-2000. Total variance was apportioned to between-city, between-tract, between-residence, and seasonal variation, as well as measurement uncertainty using variance component analysis and log-transformed data for frequently detected compounds. Outdoors, seasonal variation was the greatest portion (44-67%) of total variance, and city effects were significant (19-24%). Indoors, seasonality dominated variability of PAH measurements (>50%). Gas-phase PAHs varied more within city than between cities; particulate-phase PAHs varied significantly between cities but were largely homogeneous within cities. Gas-phase chlordanes showed larger intra-urban variation (63%) than seasonal variation (18%). Measurement uncertainty was generally below 10% with a few exceptions occurring at very low concentrations. Results indicate a need to collect multiple-season samples to account for the large temporal variation between seasons. Samples from centrally located monitoring stations could be representative of ambient SVOCs. Variance component analysis is useful to weigh influential factors in SVOC concentrations, identify and apportion sources, evaluate method performance, and design effective monitoring programs.

Levels, temporal-spatial variations, and sources of organochlorine pesticides in ambient air of Lake Chaohu, China.

The residual levels of OCPs in the gas phase and particle phase in Lake Chaohu, China, were measured using GC-MS from March 2010 to February 2011. The temporal-spatial variations and sources of OCPs were also analyzed. Twenty types of OCPs were detected in the gas phase with a total concentration of 484.8 ± 550.4 pg/m³. Endosulfan, DDTs and chlordane were the primary OCPs in the gas phase. The mean concentration of OCPs in the gas phase was significantly higher in the summer than in the winter. Seventeen types of OCPs were detected in the particle phase with a total concentration of 18.3 ± 26.1 pg/m³. DDTs were major OCPs in the particle phase. The mean concentration of OCPs in the particle phase decreased at first and then increased during the period. The potential source of the HCHs in ambient air of Lake Chaohu might come from recent lindane usage. DDTs mainly came from historical dicofol usage, and an input of DDT was observed in the spring, which may result from the present use of marine paint that contains technical DDT. Endosulfan and chlordane in the air may be due to the present use of technical endosulfan and chlordane.

Small Arctic rivers transport legacy contaminants from thawing catchments to coastal areas in Kongsfjorden, Svalbard.

Decades of atmospheric and oceanic long-range transport from lower latitudes have resulted in deposition and storage of persistent organic pollutants (POPs) in Arctic regions. With increased temperatures, melting glaciers and thawing permafrost may serve as a secondary source of these stored POPs to freshwater and marine ecosystems. Here, we present concentrations and composition of legacy POPs in glacier- and permafrost-influenced rivers and coastal waters in the high Arctic Svalbard fjord Kongsfjorden. Targeted contaminants include polychlorinated biphenyls (PCBs), hexachlorobenzene (HCB), dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs) and chlordane pesticides. Dissolved (defined as fraction filtered through 0.7 µm GF/F filter) and particulate samples were collected from rivers and near-shore fjord stations along a gradient from the heavily glaciated inner fjord to the tundra-dominated catchments at the outer fjord. There were no differences in contaminant concentration or pattern between glacier and tundra-dominated catchments, and the general contaminant pattern reflected snow melt with some evidence of pesticides released with glacial meltwater. Rivers were a small source of chlordane pesticides, DDTs and particulate HCB to the marine system and the particle-rich glacial meltwater contained higher concentrations of particle associated contaminants compared to the fjord. This study provides rare insight into the role of small Arctic rivers in transporting legacy contaminants from thawing catchments to coastal areas. Results indicate that the spring thaw is a source of contaminants to Kongsfjorden, and that expected increases in runoff on Svalbard and elsewhere in the Arctic could have implications for the contamination of Arctic coastal food-webs.

Metabolomic profiling to assess the effects of chlordanes and its bioaccumulation characteristics in chicken embryo.

Although chlordane-related compounds (CHLs) have been regulated, a variety of CHLs are still identified and detected in wild birds and eggs. Embryo is one of fragile periods and is very susceptible to toxic effects of pollutants. In this study, the fate of CHLs during embryo development and degradation of CHLs in neonatal chick were investigated. During embryo development, CHLs were mainly distributed to the liver and muscle, in which trans-nonachlor and an octachlorochlordane (MC5) were hardly metabolized and showed the high persistence, implying a greater risk to birds' offspring. CHLs with the lower Kow were found to be higher uptake efficiency in embryo, implying contaminants with the lower lipophilicity may contribute to their transport to embryo. Furthermore, the effects of CHLs on the metabolome of neonatal chicks was evaluated. The ether lipid metabolism and glycerophospholipid metabolism were found to be significantly affected, which may disturb the angiogenesis and endothelial cell migration in embryogenesis. Taken together, the lipophilicity of contaminants might be a main factor influencing their transport to embryo, and metabolomics results improve understanding of the effects of CHLs on embryo.